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Electroporation-mediated transfer of plasmids to the lung results in reduced TLR9 signaling and inflammation.

Electroporation-mediated transfer of plasmids to the lung results in reduced TLR9 signaling and inflammation. Research Abstract Details 

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  • Electroporation-mediated transfer of plasmids to the lung results in reduced TLR9 signaling and inflammation. Abstract Text:

    r zhouR Zhou,j e nortonJ E Norton,n zhangN Zhang,d a deanD A Dean,

    Electroporation can deliver DNA efficiently and safely to tissues in live animals, including the lung where it causes little inflammation or lung injury. In contrast, cationic lipid-mediated gene transfer has been shown to induce an inflammatory response caused by unmethylated plasmid CpG residues, which activate the toll-like receptor (TLR9) signaling pathway. As TLR9 is located in the endosomal/lysosomal compartment, we hypothesized that plasmids do not activate TLR9 during electroporation because they enter the cytoplasm directly through transient pores in the plasma membrane. To test this, plasmids were transfected into kidney epithelial cells overexpressing TLR9 (HEK293-TLR9+) and cells lacking TLR9 (HEK293-TLR9-null). Interleukin (IL)-8 expression, an indicator of TLR9 activation, increased more than 10-fold at 24 h post-liposome transfection in HEK293-TLR9+ cells, but showed no significant increase in electroporated cells, compared with untransfected cells. In vivo liposome-mediated gene transfer caused increases in IL-6, IL-12, tumor necrosis factor alpha and interferon gamma in mouse bronchial alveolar lavage fluid, whereas the levels of these cytokines were more than 10-fold lower by comparison following electroporation. Depletion of alveolar macrophages suggested that this inflammatory response is mediated by resident pulmonary epithelial cells. These results suggest that electroporation-mediated gene transfer bypasses the TLR-9 pathway, thus accounting for the low levels of inflammation seen with this approach.

    Electroporation-mediated transfer of plasmids to the lung results in reduced TLR9 signaling and inflammation. Publishing Authors By Initials

    r zhouR Zhou,je nortonJE Norton,n zhangN Zhang,da deanDA Dean,

    For similar proteins: dna-binding proteins: toll-like receptor 9 research abstracts see: proteins: dna-binding proteins: toll-like receptor 9 research

    PUBMED ID PMID:

    MEDLINE DATE:

    Electroporation-mediated transfer of plasmids to the lung results in reduced TLR9 signaling and inflammation. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Gene therapy

    VOLUME: 14

    Page Numbers: 775-80

    Journal Abbreviation:

    ISSN: 0969-7128

    DAY: 8

    MONTH: 03

    YEAR: 2007

    Electroporation-mediated transfer of plasmids to the lung results in reduced TLR9 signaling and inflammation. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9421525

    Electroporation-mediated transfer of plasmids to the lung results in reduced TLR9 signaling and inflammation. Keywords Mesh Terms:

    KEYWORDS: Toll-Like Receptor 9

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Electroporation-mediated transfer of plasmids to the lung results in reduced TLR9 signaling and inflammation. Information

    Substance Name: DNA

    Registry Number: 9007-49-2

    Grant and Affiliation Information for Electroporation-mediated transfer of plasmids to the lung results in reduced TLR9 signaling and inflammation.

    AFFILIATION: Division of Pulmonary and Critical Care Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NHLBI

    GRANT: HL81148

    ACRONYM: HL

    MEDLINETA: Gene Ther

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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